Antimicrobial quaternary ammonium organosilane coatings

• US 20050008613A1
• Filed: 05/19/2004
• Published: 01/13/2005
• Est. Priority Date: 05/22/2003
• Status: Abandoned Application

• Current Assignee: Qore Systems LLC
• Original Assignee: Coating Systems Laboratories, Inc.
• Inventors: Peterson, William, Berman, Renee E.
• Application Number:
  US10/850,121
• Publication Number:
  US 20050008613A1
• Time in Patent Office: Days
• US Class Current: 424/78.270
• CPC Class Codes: A01N 25/10 Macromolecular compounds
• CPC Class Codes: A01N 55/00 Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing organo-phosphorus compounds A01N57/00
• CPC Class Codes: A23L 3/3463 Organic compounds; Microorganisms; Enzymes
• CPC Class Codes: A23L 3/358 Inorganic compounds
• CPC Class Codes: A23V 2002/00 Food compositions, function of food ingredients or processes for food or foodstuffs
• CPC Class Codes: C02F 1/50 by addition or application of a germicide or by oligodynamic treatment C02F1/4606, C02F1/467, C02F1/76 take precedence
• CPC Class Codes: C02F 2303/04 Disinfection

Abstract

The present invention provides novel solid phase carriers coated with a quaternary ammonium organosilane coating for use in reducing or eliminating the viable number of microorganisms in a liquid. The invention is useful in a wide variety applications, such as water purification and reduction of harmful microorganisms in liquid foodstuffs.

Claims

1. A method of reducing or eliminating the viable number of microorganisms in a liquid, said method comprising contacting said liquid with a solid phase carrier coated with a quaternary ammonium organosilane coating.

2. A method in accordance with claim 1 in which said quaternary organosilane coating is produced from a quaternary ammonium organosilane reagent having the formula:

3. A method in accordance with claim 1 in which

A is a member independently selected from the group consisting of —

OR⁴, substituted or unsubstituted (C₁-C₁₀)alkyl, substituted or unsubstituted 2 to 10 membered heteroalkyl, substituted or unsubstituted (C₅-C₇)cycloalkyl, substituted or unsubstituted 5 to 7 membered heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl;

wherein R⁴ is a member selected from the group consisting of hydrogen, substituted or unsubstituted (C₁-C₁₀)alkyl, substituted or unsubstituted 2 to 10 membered heteroalkyl, substituted or unsubstituted (C₅-C₇)cycloalkyl, substituted or unsubstituted 5 to 7 membered heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl;

R is a member selected from the group consisting of substituted or unsubstituted (C₁-C₁₀) alkylene, substituted or unsubstituted 2 to 10 membered heteroalkyene, substituted or unsubstituted (C₅-C₇)cycloalkyene, substituted or unsubstituted 5 to 7 membered heterocycloalkylene, substituted or unsubstituted arylene, and substituted or unsubstituted heteroarylene; and

R¹, R², and R³ are members independently selected from the group consisting of hydrogen, substituted or unsubstituted (C₁-C₂₀)alkyl, substituted or unsubstituted 2 to 20 membered heteroalkyl, substituted or unsubstituted (C₅-C₇)cycloalkyl, substituted or unsubstituted 5 to 7 membered heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl.

4. A method in accordance with claim 3 in which

each substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and substituted heteroaryl are substituted only with at least one substituent independently selected from the group consisting of —

OH, unsubstituted (C₁-C₅)alkyl, unsubstituted 2 to 5 membered heteroalkyl, unsubstituted (C₅-C₇) membered cycloalkyl, unsubstituted 5 to 7 membered heterocycloalkyl, unsubstituted aryl, and unsubstituted heteroaryl; and

said substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and substituted heteroarylene are substituted only with at least one substituent independently selected from the group consisting of —

OH, unsubstituted (C₁-C₅)alkyl, unsubstituted 2 to 5 membered heteroalkyl, unsubstituted (C₅-C₇) membered cycloalkyl, substituted 5 to 7 membered heterocycloalkyl, unsubstituted aryl, and unsubstituted heteroaryl.

5. A method in accordance with claim 3 in which

each substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and substituted heteroaryl are substituted only with at least one substituent independently selected from the group consisting of—

OH, unsubstituted (C₁-C₅)alkyl, unsubstituted (C₅-C₇) membered cycloalkyl, and unsubstituted phenyl; and

said substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and substituted heteroarylene are substituted only with at least one substituent independently selected from the group consisting of —

OH, unsubstituted (C₁-C₅)alkyl, unsubstituted (C₅-C₇) membered cycloalkyl, and unsubstituted phenyl.

6. A method in accordance with claim 3 in which

each substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and substituted heteroaryl are substituted only with at least one unsubstituted (C₁-C₃)alkyl;

and

said substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and substituted heteroarylene are substituted only with at least one (C₁-C₃)alkyl.

7. A method in accordance with claim 3 in which

A is a member independently selected from the group consisting of —

OR⁴, unsubstituted (C₁-C₁₀)alkyl, unsubstituted 2 to 12 membered heteroalkyl, unsubstituted (C₅-C₇)cycloalkyl, unsubstituted 5 to 7 membered heterocycloalkyl, unsubstituted aryl, and unsubstituted heteroaryl,

wherein R⁴ is a member selected from the group consisting of hydrogen, unsubstituted (C₁-C₁₀)alkyl, unsubstituted 2 to 12 membered heteroalkyl, unsubstituted (C₅-C₇)cycloalkyl, unsubstituted 5 to 7 membered heterocycloalkyl, unsubstituted aryl, and unsubstituted heteroaryl;

R is a member selected from the group consisting of unsubstituted (C₁-C₁₀)alkylene, unsubstituted 2 to 10 membered heteroalkylene, unsubstituted (C₅-C₇)cycloalkylene, unsubstituted 5 to 7 membered heterocycloalkylene, unsubstituted arylene, and unsubstituted heteroarylene;

R¹, R², and R³ are members independently selected from the group consisting of hydrogen, unsubstituted (C₁-C₂₀)alkyl, hydroxy-substituted (C₁-C₂₀)alkyl, amine-substituted (C₁-C₂₀)alkyl, unsubstituted 2 to 20 membered heteroalkyl, unsubstituted (C₅-C₇)cycloalkyl, unsubstituted 5 to 7 membered heterocycloalkyl, unsubstituted aryl, and unsubstituted heteroaryl.

8. A method in accordance with claim 3

A is a member independently selected from the group consisting of —

OR⁴, unsubstituted (C₁-C₁₀)alkyl, unsubstituted 3 to 12 membered alkylether, unsubstituted (C₅-C₇)cycloalkyl, and unsubstituted phenyl,

wherein R⁴ is a member selected from the group consisting of hydrogen, unsubstituted (C₁-C₁₀)alkyl, unsubstituted 3 to 12 membered alkylether, unsubstituted (C₅-C₇)cycloalkyl, and unsubstituted phenyl;

R is unsubstituted (C₁-C₁₀)alkylene;

R¹, R², and R³ are members independently selected from the group consisting of hydrogen, unsubstituted (C₁-C₂₀)alkyl, unsubstituted alkylether, hydroxy-substituted (C₁-C₂₀)alkyl, amine-substituted (C₁-C₂₀)alkyl, unsubstituted (C₅-C₇)cycloalkyl, and unsubstituted phenyl.

9. A method in accordance with claim 3 in which

A is a member independently selected from the group consisting of —

OR⁴, unsubstituted (C₁-C₄)alkyl, unsubstituted 3 to 8 membered alkylether, unsubstituted (C₅-C₇)cycloalkyl, and unsubstituted phenyl,

wherein R⁴ is a member selected from the group consisting of hydrogen, unsubstituted (C₁-C₈)alkyl, unsubstituted 3 to 8 membered alkylether, unsubstituted (C₅-C₇)cycloalkyl, and unsubstituted phenyl;

R is unsubstituted (C₁-C₁₀)alkylene;

R¹, R², and R³ are members independently selected from the group consisting of hydrogen, unsubstituted (C₁-C₂₀)alkyl, unsubstituted alkylether, hydroxy-substituted (C₁-C₂₀)alkyl, amine-substituted (C₁-C₂₀)alkyl, unsubstituted (C₅-C₇)cycloalkyl, and unsubstituted phenyl.

10. A method in accordance with claim 3 in which

A is a member independently selected from the group consisting of —

OR⁴, unsubstituted (C₁-C₄)alkyl, and unsubstituted 3 to 8 membered alkylether,

wherein R⁴ is a member selected from the group consisting of hydrogen, unsubstituted (C₁-C_{8 )alkyl, and unsubstituted} 3 to 8 membered alkylether;

R is unsubstituted (C₁-C₁₀)alkylene;

R¹, R², and R³ are members independently selected from the group consisting of hydrogen, unsubstituted (C₁-C₂₀)alkyl, unsubstituted alkylether, hydroxy-substituted (C₁-C₂₀)alkyl, and amine-substituted (C₁-C₂₀)alkyl.

11. A method in accordance with claim 10 in which R¹, R², and R³ are members independently selected from the group consisting of —

(CH₂)_qOCH₃, —

(CH₂)_qOH, —

(CH₂)_qO(CH₂)_tCH₃, —

CH₂)_qNHCH₃, —

(CH₂)_qNH₂, —

(CH₂)_qN(CH₃)₂ and —

(CH₂)_qNH₂(CH₂)_tCH₃, wherein q and t are integers independently selected from 0 to 10.

12. A method in accordance with claim 10 in which R¹, R², and R³ are members independently selected from the group consisting of —

CH₂CH₂OCH₃ and —

CH₂CH₂OCH₂CH₂CH₃.

13. A method in accordance with claim 10 in which R¹, R², and R³ are members independently selected from the group consisting of —

CH₂CH₂OH and —

CH₂CH₂CH₂CH(OH)CH₃.

14. A method in accordance with claim 10 in which R¹, R², and R³ are members independently selected from the group consisting of —

CH₂CH₂NH₂ and —

CH₂CH₂N(CH₃)₂.

15. A method in accordance with claim 10 in which R¹, R², and R³ are members independently selected from the group consisting of methyl, octadecyl, didecyl, and tetradecyl.

16. A method in accordance with claim 2 in which said quaternary ammonium organosilane reagent is 3-(trimethoxysilyl)propyldimethyloctadecyl ammonium chloride.

17. A method in accordance with claim 2 in which said quaternary ammonium organosilane reagent is 3-(trimethoxysilyl)propyldidecylmethyl ammonium chloride.

18. A method in accordance with claim 2 in which said quaternary ammonium organosilane reagent is 3-(trimethoxysilyl)propyldimethyltetradecyl ammonium chloride.

19. A method in accordance with claim 1 in which said liquid is contacted with at least one additional solid phase carrier coated with a different quaternary ammonium organosilane coating.

20. A method in accordance with claim 1 in which said microorganisms are member selected from the group consisting of gram-positive and gram-negative bacteria.

21. A method in accordance with claim 1 in which said microorganisms are viruses.

22. A method in accordance with claim 1 in which said microorganisms are fungi.

23. A method in accordance with claim 1 in which said microorganisms are a member selected from the group consisting of algae and mold.

24. A method in accordance with claim 1 in which said microorganisms are yeast.

25. A method in accordance with claim 1 in which said microorganisms are spores.

26. A method in accordance with claim 1 in which said liquid is a member selected from the group consisting of water and aqueous solution.

27. A method in accordance with claim 26 in which said solid phase carrier comprises a material selected from the group consisting of glass, silica, sand, quartz, flint, zeolite, anthracite, activated carbon, garnet, ilmenite, berm, non-hydrous aluminum silicate, oxides of iron and titanium, diatomaceous earth, pozzolan, metal, ceramic, and organic plastic.

28. A method in accordance with claim 1 in which said liquid is contacted with an additional solid phase carrier, wherein said additional solid phase carrier comprises a different material than said solid phase carrier.